GB2338490A - Polishing Composition - Google Patents
Polishing Composition Download PDFInfo
- Publication number
- GB2338490A GB2338490A GB9913961A GB9913961A GB2338490A GB 2338490 A GB2338490 A GB 2338490A GB 9913961 A GB9913961 A GB 9913961A GB 9913961 A GB9913961 A GB 9913961A GB 2338490 A GB2338490 A GB 2338490A
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- GB
- United Kingdom
- Prior art keywords
- polishing
- polishing composition
- abrasive
- composition
- memory hard
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09G—POLISHING COMPOSITIONS; SKI WAXES
- C09G1/00—Polishing compositions
- C09G1/02—Polishing compositions containing abrasives or grinding agents
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
- C09K3/1409—Abrasive particles per se
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
- C09K3/1454—Abrasive powders, suspensions and pastes for polishing
- C09K3/1463—Aqueous liquid suspensions
Abstract
A polishing composition for memory hard disks, which comprises water and at least one abrasive selected from the group consisting of aluminum oxide, silicon dioxide, cerium oxide, zirconium oxide, titanium oxide, silicon nitride and manganese dioxide, and which further contains succinic acid or its salt dissolved in the composition.
Description
2338490 - 1 POLISHING COMPOSITIO The present invention relates to a
polishing composition suitable for finish polishing of the surface of substrates for memory hard disks, i.e. magnetic disks to be used for memory devices used for computers, etc., in the production of such memory hard disks. More particularly, the present invention relates to a polishing composition which is useful for finish polishing of disk substrates (hereinafter referred to as "substrates") to be used for memory hard disks represented by Ni-P disks, Ni-Fe disks, aluminum disks, boron zarbide disks and carbon disks and which is applicable to a production technique, whereby it is possible to prevent formation of micro protrusions, micro is pits and other surface defects and to provide a polishing rate not lower than conventional polishing compositions, and at the same time, it is possible to obtain an excellent finished surface useful for magnetic disk devices with high capacities and high recording densities.
Memory hard disks to be used for magnetic disk 9 - 2 devices as memory media for computers, etc., tend to be small in si- ze and large in capacity year after year, and magnetic media are changing from conventional coating type media to thin film media by means of a sputtering s method, a plating method or the like.
Substrates which are most widely used at present, are ones having electroless Ni-P plating applied to a blank material. Here, a blank material is one obtained by shaping an aluminum or other base plate as a base lo material for a substrate, by lathe processing by means of a diaturn for the purpose of providing parallelism or flatness, by lapping by means of a PVA grindstone prepared by binding SiC abrasive material, or by other methods. However, by the abovementioned various shaping methods, it is not possible to completely remove relatively large waviness. Accordingly., when electroless Ni-P plating is applied to such a blank material, a film will be formed along such waviness, whereby the resulting substrate will also have the waviness. Polishing is carried out for the purpose of removing such waviness of the substrate and smoothing the surface.
Along with the increase in the capacity of memory hard disks, the area recording density is increasing at a rate of a few tens % per year. Accordingly, the space on a memory hard disk occupied by a predetermined amount of information recorded, tends to be very narrow, and the magnetic force required for recording tends to be weak.
3 Accordingly, with a recent magnetic disk device, it is required toreduce the head flying height which is the space between the magnetic head and the memory hard disk, and the head flying height has now been reduced to a s level of not higher than 0.02 pm.
Further, so-called texturing may be applied to provide a concentric texture to a substrate after polishing, for the purpose of preventing sticking to the memory hard disk of a magnetic head for reading and lo writing information, or preventing a possibility that the magnetic field on a memory hard disk becomes non-uniform due to a texture in one direction which is different from the rotational direction of the memory hard disk, formed by polishing the substrate surface. Recently, light texturing is carried out to reduce the texture provided on the substrate for the purpose of further reducing the flying height of the head, and a non-textured substrate is now being employed which has no texturing applied. A technique to support such reduction of the flying height of the magnetic head has been developed, and reduction of the flying height of the head is progressing more than ever.
A magnetic head flies along the shape of the surface of a memory hard disk which is rotated at a very high speed. If there is a micro protrusion of a level of a few pm on the memory hard disk surface, so-called "head crush" is likely to occur, and the head crushes against 4 the protrusion, whereby the magnetic head and/or the magnetic medium on the surface of the memory hard disk may be damaged, thus leading to a failure of the magnetic disk device or an error in reading or writing information.
On the other hand, if pits are present on a memory hard disk, information can not be completely written, thus leading to omission of information or failure in reading out of information, so-called "bit falls", and causing an error.
Here, "pits" are dents initially present in the substrate or dents formed on the substrate surface by polishing, and micro pits are dents having a diameter of less than about 10 lim, among them.
Accordingly, it is important to reduce the roughness on the substrate surface, and at the same time, it is necessary to completely remove relatively large waviness, micro protrusions or pits and other surface defects, in the step before forming a magnetic medium i. e. in the polishing step.
For the above-described purpose, it has been heretofore common to carry out finishing by a single polishing operation by means of a polishing composition (hereinafter referred to as a "slurry" from its nature) comprising an aluminum oxide or other various abrasives and water, and various polishing accelerators. For example, JP-B-64-436 and JP-B-2-23589 disclose a polishing composition for memory hard disks, prepared by adding and mixing aluminum nitrate, nickel nitrate or nickel sulfa-te as a polishing accelerator to water and aluminum oxide, to form a slurry. Further, JP-B-438788 discloses an acidic polishing composition for aluminum magnetic disks, which is prepared by adding gluconic acid or lactic acid as a polishing accelerator and colloidal alumina as a surface-modifier, to water and fine powder of alumina abrasive. Still further, JP-A-7- 216345 discloses a polishing composition comprising water, an lo alumina abrasive and a polishing accelerator, wherein the polishing accelerator comprises a molybdenate and an organic acid.
However, with any one of the above polishing compositions, it has been very difficult to satisfy all of the requirements for removing relatively large waviness and surface defects on a substrate surface, finishing to reduce the surface roughness to a very low level in a predetermined period of time and preventing formation of micro protrusions, micro pits and other surface defects, in a single step of polishing. Accordingly, a polishing process comprising at least two steps has now been studied.
To carry out a polishing process in two steps, it is the main purpose of polishing in the first step to remove the relatively large waviness, large pits and other surface defects on the substrate surface, i.e. to carry out fairing or reshaping. Accordingly, a polishing 1 1-1 - 6 composition is required which has a high ability to process and-mend the above-mentioned waviness or surface defects with little formation of deep scratches which can not be removed by finish polishing in the second step, 5 rather than to reduce the surface roughness.
The purpose of polishing in the second step i.e. finish polishing is to minimize the surface roughness of the substrate. For this purpose, it is important for a polishing composition to be able to reduce the surface roughness and to prevent formation of micro protrusions, micro pits and other surface defects, rather than to have a high ability to process or mend a large waviness or surface defects as required for polishing in the first step. Further, from the viewpoint of the productivity, is it is also important that the polishing rate is high. As far as the present inventors are aware,. it is possible to obtain a substrate surface having small surface roughness in polishing in the second step by a conventional two step polishing, but the polishing rate is very low and inadequate for practical production, or it has been difficult to prevent formation of micro protrusions, micro pits or other surface defects.
The degree of surface roughness is determined by the process for preparing the substrate, the final memory capacity as the memory hard disk, and other conditions, and depending upon the degree of the desired surface roughness, a polishing process comprising more than two 1 I- 7 steps may be employed.
it is an object of the present invention to solve the above-described problems and to provide a polishing composition which is capable of preventing formation of micro protrusions, micro pits and other surface defects with a polishing rate not lower than conventional polishing compositions, in finish polishing of a substrate to be used for a memory hard disk, and which, at the same time, is capable of obtaining an excellent finished surface which is useful for a magnetic disk device with a high capacity and a high memory density.
The present invention provides a polishing composition for memory hard disks, which comprises water and at least one abrasive selected from the group is consisting of aluminum oxide, silicon dioxide, cerium oxide, zirconium oxide, titanium oxide,. silicon nitride and manganese dioxide, and which further contains succinic acid or its salt dissolved in the composition.
The polishing composition of the present invention is capable of preventing formation of micro protrusions, micro pits and other surface defects with a polishing rate not lower than conventional polishing compositions, in finish polishing of a substrate to be used for a memory hard disk and, at the same time, capable of obtaining an excellent finished surface.
The average particle size of the abrasive is preferably less than 0.5 gm, more preferably not more than 0.4 gm.
Now, the present invention will be described in detailed with reference to the preferred embodiments.
Abrasive The abrAsive suitable for use as the main abrasive among various components of the polishing composition of the present invention, is selected from the group consisting of aluminum oxide, silicon dioxide, cerium oxide, zirconium oxide, titanium oxide, silicon nitride and manganese dioxide. Aluminum oxide includes a alumina, 6 -alumina, 0 alumina, K -alumina and other morphologically different substances. Further, there is one called fumed alumina from the method of its preparation.
Silicon dioxide includes colloidal silica, fumed silica and many other different types which differ in the nature or the method of preparation.
Cerium oxide includes trivalent one and tetravalent one from the oxidation number, and it includes hexagonal system, regular system and face-centered cubic system, from the crystal system.
zirconium oxide includes monoclinic system, tetragonal system and amorphous one from the crystal system. Further, there is one called fumed zirconia from the method of its preparation.
Titanium oxide includes titanium monoxide, dititanium trioxide, titanium dioxide and others, from the crystal system.. Further, there is one called fumed titania from the method of its preparation.
Silicon nitride includes a-silicon nitride, 1 9 silicon nitride, amorphous silicon nitride and other morphologically different substances.
Manganese dioxide includes a -manganese dioxide, manganese dioxide, y manganese dioxide, 6 -manganese dioxide, E -manganese dioxide, 77 manganese dioxide and others from the morphology.
For the composition of the present invention, these abrasives may be used optionally or in an optional combination, as the case requires. When they are used in combination, the particular combination or the ratio is not particularly limited. The above abrasives are ones which polish the surface to be polished by a mechanical action as abrasive grains. The particle size of silicon dioxide among them is 15 usually from 0.005 to 0. 5 11m, preferably from 0.01 to 0.2 lim, as an average particle size obtained from the surface area measured by a BET method. Likewise, the particle size of aluminum oxide, zirconium oxide, titanium oxide, silicon nitride or manganese dioxide, is usually from 20 0.005 to 0.5 pm, preferably from 0.05 to 0.5 pm, as an average particle size obtained from the surface area measured by a BET method. Further, the particle size of cerium oxide is usually from 0.01 to 0.5 gm, preferably from 0.05 to 0.45 pm, as an average particle size observed by a scanning electron microscope. If the average particle sizes of these abrasives exceed the respective ranges as shown above, there may - 10 be a problem such that the surface roughness of the polished surface will be large, or scratches are likely to form. on the other hand, if they are smaller than the respective ranges, the polishing rate tends to be very low, such being not practical.
The content of the abrasive in the polishing composition is usually from 0.1 to 50 wt%, preferably from 1 to 25 wt%, based on the total amount of the composition. If the content of the abrasive is too small, io micro protrusions or micro pits, and other surface defects, tend to form, and the polishing rate is likely to be low. on the other hand, if it is too large, uniform dispersion tends to hardly be maintained, and the viscosity of the composition tends to be excessive, whereby handling is likely to be difficult. Succinic acid or its salt The polishing composition of the present invention further contains succinic acid or its salt. In the polishing composition of the present invention, succinic acid accelerates the polishing action by a chemical action, as a polishing accelerator. Succinic acid or its salt to be used may be any optional one so long as it can be dissolved in the composition. Specifically, it may, for example, be succinic acid, sodium succinate, potassium succinate or ammonium succinate.
The content of succinic acid or its salt in the polishing composition of the present invention varies - 11 depending upon the type of succinic acid or its salt, but it is prefe-rably from 0.01 to 10 wt%, more preferably from 0.05 to 5 wt%, most preferably from 0.1 to 3 wt%, based on the total amount of the polishing composition. As the amount of succinic acid or its salt increases, the polishing rate tends to increase, and formation of micro pits tends to decrease. However, even if the amount is increased excessively, no stronger effect of the present invention is likely to be obtainable, and an economical lo demerit is likely to result. on the other hand, if the amount is too small, it will be difficult to adequately prevent formation of micro protrusions, micro pits and other surface defects, and no adequate polishing rate tends to be obtainable.
Alumina sol The polishing composition of the present invention may further contain alumina sol. Alumina sol for the purpose of the present invention is one having hydrated alumina or aluminum hydroxide dispersed in an acidic aqueous solution in a colloidal state. Hydrated alumina includes boehmite, pseudo boehmite, diaspore, gypsite, bialite and others. The alumina sol to be used for the composition of the present invention is particularly preferably one having boehmite or pseudo boehmite dispersed in an acidic aqueous solution.
The content of the alumina sol in the polishing composition of the present invention is preferably from - 12 0.01 to 20 wt%, more preferably from 0.05 to 15 wt%, most preferably from 0.1 to 10 wt%, based on the total amount of the composition. As the amount of the alumina sol is increased, formation of micro pits and other surface defects tends to decrease. However, even if the amount is increased excessively, no further effect of the present invention may be obtained, and an economical demerit is likely to result. Polishing composition The polishing composition of the present invention is prepared usually by mixing and dispersing an abrasive selected from the group consisting of aluminum oxide, silicon dioxide, cerium oxide, zirconium oxide, titanium oxide, silicon nitride and manganese dioxide in water in an optional content, and further dissolving succinic acid or its salt. If necessary, alumina sol. may further be mixed and dispersed to this slurry. The method of dispersing or dissolving these components in water, is optional. For example, they may be dispersed by ultrasonic dispersion or stirring by a vane type stirrer.
Further, order of mixing them is optional, and dispersion of the abrasive, dissolution of succinic acid or its salt, and mixing and dispersing alumina sol when used, may be carried out in any order, or simultaneously.
Further, various known additives may further be incorporated for the purpose of stabilizing or maintaining the quality of the product, or as required - 13 depending upon the type of the object to be polished, the condition fbr polishing and other requirements for polishing.
The following may be mentioned as suitable examples of such further additives: (a) celluloses, such as cellulose, carboxymethyl cellulose, hydroxyethyl cellulose and others, (b) water-soluble alcohols such as ethanol, propanol, ethylene glycol and others, (c) surfactants such as a sodium alkylbenzenesulfonate, a formalin condensate of naphthalene sulfonic acid, and others, (d) organic polyanionic substances, such as sodium lignin sulfonate, polyacrylate and others, is (e) watersoluble polymers (emulsifiers), such as polyvinyl alcohol and others, (f) chelating agents such as dimethyl glyoxime, dithizone, oxine, acetylacetone, glycine, EDTA, NTA and others, and (g) fungicides, such as sodium alginate, potassium hydrogencarbonate and others.
Further, the above abrasive, succinic acid or its salt, and optional alumina sol, suitable for use in th polishing composition of the present invention, may be employed as auxiliary additives for the purpose other than the above-mentioned purpose, e.g. for preventing sedimentation of the abrasive.
Further, the polishing composition of the present 1 - 14 invention may be prepared and stored or transported in the form of-a stock solution having a relatively high concentration, so that it may be diluted for use at the time of actual polishing operation. The above- mentioned preferred concentration ranges are those for the practical polishing operation. It is needless to say that in a case where the composition is diluted at the time of actual use, it is in the form of a solution having a high concentration when it is stored or transported. Further, from the viewpoint of the handling efficiency, it is preferably prepared in such a concentrated form.
JP-B-4-38788 describes that even if succinic acid is added to a polishing composition comprising water, aluminum oxide having an average particle size of from 0.5 to 15 11m and alumina sol, it is not possible to prevent formation of micro protrusions, micro pits and other surface defects in the polishing operation. In view of this description, it is surprising that the polishing composition of the present invention is capable of preventing formation of such surface defects. The detailed mechanism has not yet been known, but the following explanation may be made taking a Ni-P plated substrate as an example.
Firstly, with respect to the reason why formation of micro protrusions, micro pits and other surface defects can be prevented, succinic acid or its salt has an action - is - to accelerate the mechanical polishing effect of the abrasive, ahd effectively acts against relatively small particles, although the action may not be adequate against large abrasive particles. This action tends to be enhanced by an addition of alumina sol. This is considered attributable to the fact that the alumina sol adheres to the surface of the abrasive in the composition or is dispersed among the abrasive particles in the composition in a colloidal state and thus has a function lo to create an excellent dispersed state of the abrasive, and it acts especially effectively against relatively small abrasive particles.
On the other hand, with respect to a reason why an excellent polished surface having a small surface roughness, can be obtained, it is considered that by the use of an abrasive having a relatively-small average particle size and by the effect of succinic acid or its salt as described above, micro protrusions, micro pits and other surface defects can hardly be formed, and a smooth surface to be coated which is free from scratch marks, can be obtained.
Further, in a case where the polishing composition of the present invention contains alumina sol, the alumina sol deposits on the surface of abrasive particles in the composition and thereby accelerates the mechanical polishing action of the abrasive, whereby micro protrusions, micro pits and other surface defects on the - 16 surface to be polished, can be prevented. Further, it is dispersed in- a colloidal state among the abrasive particles in the composition thereby to provide a function to prevent the abrasive from settling down firmly, and it also has a function to adjust the viscosity of the composition or to let the abrasive particles be readily maintained on a pad.
Now, the polishing composition of the present invention will be described in further detail with reference to Examples. However, it should be understood that the present invention is by no means restricted to such specific Examples. Preparation of polishing cQm12ositions Firstly, as an abrasive, aluminum oxide as identified in Table 1 was dispersed in water by means of a stirrer to obtain a slurry having an abrasive concentration of 10 wt%. on the other hand, to an aqueous solution containing 1 wt% of succinic acid, 10 wt% of boehmite alumina hydrate was added and dispersed in a colloidal state by means of a homogenizer to obtain an alumina sol.
The slurry and water were mixed, and, as the case requires, the alumna sol or other additives were added, to prepare samples of Examples 1 to 4 and Comparative Examples 1 to 3.
Preiparation of substrates for DQlishina tests To carry out polishing tests using the abovementioned polishing compositions, substrates were 17 prepared. To carry out evaluation by two step polishing, firstly, tet substrates were prepared as follows.
Polishina conditions (first step) object to be polished: 3.5 inch electroless Ni-P plated substrate Number of sheets polished: 10 sheets Polishing machine: Both side polishing machine (surface table diameter: 640 mm) Polishing pad: Politex DG (manufactured by Rodel Inc., U.S.A.) Polishing pressure: 80 g/cm 2 Rotational speed of surface table: 60 rpm Polishing composition: DISKLITE3471 (manufactured by FUJIMI INCORPORATED) Dilution of the composition: 1:2 pure water Amount of the polishing composition supplied:
cc/min Polishing time: 5 minutes Polishing test Then, using the substrate polished in the first step with the above polishing composition, a polishing test was carried out under the following conditions:
Polishing conditions (second step) Object to be polished: 3.5 inch electroless Ni-P plated substrate (polished in the first step) Number of sheets polished: 15 sheets 1' - 18 Polishing machine: Both side polishing machine (surface table diameter: 700 mm) Polishing pad: Politex DG (manufactured by Rodel Inc., U.S.A.) 2 Polishing pressure: 60 g/CM Rotational speed of surface table: 60 rpm Amount of the polishing composition supplied:
cc/min Polishing time: 5 minutes After the polishing, the substrate was sequentially washed and dried, whereupon the weight reduction of the substrate by polishing was measured, and from the average of such weight reduction, the polishing rate was obtained. Further, by means of a differential interference microscope (400 magnifications), the substrate surface was observed, and presence or absence of formation of micro pits was measured. The evaluation standards were as follows. Micro pits were not visually observed.
0: Micro pits were not substantially visually observed.
X: micro pits were substantially visually observed and were a problematic level.
The obtained results were as shown in Table 1.
- 19 Table 1
Average Amount Alumina Polishing Micro Example No. particle. Additive rate size (pm) (wt%) sol (wt%) (pm/min) pits 1 0.25 Succinic acid 1 3 0.20 0 2 0.25 Succinic acid 3 - 0.23 0 3 0.25 Succinic acid 3 3 0.23 4 0.25 Succinic acid 10 3 0.24 Comparative 1 0.70 Succinic acid 3 3 0.35 X Comparative 2 0.25 Gluconic acid 3 3 0.24 X Comparative 3 0.25 Lactic acid 3 3 0.22 X 1 1 ko 1 I,' From the results shown in Table 1, it is evident that when the polishing compositions of the present invention are used for surface polishing of substrates, excellent polished surfaces are obtainable with little formation of micro pits and with a polishing rate not lower than conventional polishing compositions.
As described in the foregoing, the polishing composition of the present invention is capable of preventing formation of micro pits and other surface lo defects with a polishing rate not lower than conventional polishing compositions, in finish polishing of substrates to be used for memory hard disks, and capable of forming excellent polished surfaces.
Claims (11)
- - 21 CLAIMS: 1. A polishing composition for memory hard disks, whichcomprises water and at least one abrasive selected from the group consisting of aluminum oxide, silicon dioxide, cerium oxide, zirconium oxide, titanium oxide, silicon nitride and manganese dioxide, and which further contains succinic acid or its salt dissolved in the composition.
- 2. The polishing composition according to Claim 1, which further contains aluminum hydroxide.
- 3. The polishing composition according to Claim 1 or 2, wherein the abrasive is at least one abrasive selected from the group consisting of aluminum oxide, silicon dioxide, zirconium oxide, titanium oxide, silicon nitride and manganese dioxide, and the average particle size of the abrasive obtained from the surface area measured by a BET method, is from 0.005 to 0.5 m..
- 4. The polishing composition according to Claim 1 or 2, wherein the abrasive is cerium oxide, and the average particle size of the abrasive observed by a scanning electron microscope, is from 0.01 to 0.5 lim.
- 5. The polishing composition according to any one of Claims 1 to 4, wherein the content of the abrasive is from 0.1 to 50 wt%, based on the weight of the polishing composition.
- 6. The polishing composition according to any one of Claims 1 to 5, wherein the content of succinic acid or its salt is from 0.01 to 10 wt%, based on the weight of 22 - the polishing composition.
- 7. The polishing composition according to any one of Claims 2 to 6, wherein the content of aluminum hydroxide is from 0. 01 to 20 wt%, based on the weight of the polishing composition.
- 8. Use of the polishing composition as defined in any one of Claims 1 to 7 as a composition for polishing memory hard disks.
- 9. A method for polishing memory hard disks, wherein the lo polishing composition as defined in any one of Claims 1 to 7 is used as a composition for polishing memory hard disks.
- 10. A method according to claim 9 wherein the polishing composition is used in a finishing polishing step in a polishing process of a memory hard disk substrate having at least two polishing steps.
- 11. A polishing composition for memory hard disks according to claim 1 substantially as any herein described in the Examples.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0307529A GB2384003B (en) | 1998-06-15 | 1999-06-15 | Polishing composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16675698A JP3998813B2 (en) | 1998-06-15 | 1998-06-15 | Polishing composition |
Publications (3)
Publication Number | Publication Date |
---|---|
GB9913961D0 GB9913961D0 (en) | 1999-08-18 |
GB2338490A true GB2338490A (en) | 1999-12-22 |
GB2338490B GB2338490B (en) | 2003-08-06 |
Family
ID=15837153
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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GB9913961A Expired - Fee Related GB2338490B (en) | 1998-06-15 | 1999-06-15 | Polishing composition |
Country Status (9)
Country | Link |
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US (1) | US6193790B1 (en) |
JP (1) | JP3998813B2 (en) |
KR (1) | KR20000006122A (en) |
CN (2) | CN1240798C (en) |
GB (1) | GB2338490B (en) |
IE (1) | IE990498A1 (en) |
MY (1) | MY116322A (en) |
SG (1) | SG75964A1 (en) |
TW (1) | TW500793B (en) |
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CN113549424B (en) * | 2021-08-04 | 2022-05-13 | 白鸽磨料磨具有限公司 | Cerium oxide cluster powder for polishing and preparation method thereof |
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Publication number | Priority date | Publication date | Assignee | Title |
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US4956015A (en) * | 1988-01-19 | 1990-09-11 | Mitsubishi Kasei Corporation | Polishing composition |
JPH0781132B2 (en) * | 1990-08-29 | 1995-08-30 | 株式会社フジミインコーポレーテッド | Abrasive composition |
EP0786504A3 (en) * | 1996-01-29 | 1998-05-20 | Fujimi Incorporated | Polishing composition |
US5858813A (en) * | 1996-05-10 | 1999-01-12 | Cabot Corporation | Chemical mechanical polishing slurry for metal layers and films |
US5993686A (en) * | 1996-06-06 | 1999-11-30 | Cabot Corporation | Fluoride additive containing chemical mechanical polishing slurry and method for use of same |
US5783489A (en) * | 1996-09-24 | 1998-07-21 | Cabot Corporation | Multi-oxidizer slurry for chemical mechanical polishing |
US5954997A (en) * | 1996-12-09 | 1999-09-21 | Cabot Corporation | Chemical mechanical polishing slurry useful for copper substrates |
US6309560B1 (en) * | 1996-12-09 | 2001-10-30 | Cabot Microelectronics Corporation | Chemical mechanical polishing slurry useful for copper substrates |
US6063306A (en) * | 1998-06-26 | 2000-05-16 | Cabot Corporation | Chemical mechanical polishing slurry useful for copper/tantalum substrate |
-
1998
- 1998-06-15 JP JP16675698A patent/JP3998813B2/en not_active Expired - Lifetime
-
1999
- 1999-06-01 SG SG1999002833A patent/SG75964A1/en unknown
- 1999-06-04 US US09/325,393 patent/US6193790B1/en not_active Expired - Fee Related
- 1999-06-11 MY MYPI99002397A patent/MY116322A/en unknown
- 1999-06-11 TW TW088109830A patent/TW500793B/en not_active IP Right Cessation
- 1999-06-11 KR KR1019990021803A patent/KR20000006122A/en not_active Application Discontinuation
- 1999-06-15 CN CNB031009956A patent/CN1240798C/en not_active Expired - Fee Related
- 1999-06-15 CN CN99108657A patent/CN1129656C/en not_active Expired - Fee Related
- 1999-06-15 IE IE19990498A patent/IE990498A1/en not_active IP Right Cessation
- 1999-06-15 GB GB9913961A patent/GB2338490B/en not_active Expired - Fee Related
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001074959A2 (en) * | 2000-04-04 | 2001-10-11 | Cabot Microelectronics Corporation | Method for polishing a memory or rigid disk with an amino acid-containing composition |
WO2001074959A3 (en) * | 2000-04-04 | 2002-07-04 | Cabot Microelectronics Corp | Method for polishing a memory or rigid disk with an amino acid-containing composition |
US6471884B1 (en) | 2000-04-04 | 2002-10-29 | Cabot Microelectronics Corporation | Method for polishing a memory or rigid disk with an amino acid-containing composition |
MY119974A (en) * | 2000-04-04 | 2005-08-30 | Cabot Microelectronics Corp | Method for polishing a memory or rigid disk with an amino acid-containing composition |
GB2393447A (en) * | 2002-08-07 | 2004-03-31 | Kao Corp | Polishing composition |
US6902591B2 (en) | 2002-08-07 | 2005-06-07 | Kao Corporation | Polishing composition |
GB2393447B (en) * | 2002-08-07 | 2006-04-19 | Kao Corp | Polishing composition |
GB2401370A (en) * | 2003-05-09 | 2004-11-10 | Fujimi Inc | Polishing composition |
GB2401370B (en) * | 2003-05-09 | 2007-12-05 | Fujimi Inc | Polishing composition |
Also Published As
Publication number | Publication date |
---|---|
CN1239129A (en) | 1999-12-22 |
CN1515640A (en) | 2004-07-28 |
CN1240798C (en) | 2006-02-08 |
JP2000001665A (en) | 2000-01-07 |
GB9913961D0 (en) | 1999-08-18 |
KR20000006122A (en) | 2000-01-25 |
US6193790B1 (en) | 2001-02-27 |
JP3998813B2 (en) | 2007-10-31 |
IE990498A1 (en) | 2000-11-15 |
TW500793B (en) | 2002-09-01 |
MY116322A (en) | 2003-12-31 |
SG75964A1 (en) | 2000-10-24 |
GB2338490B (en) | 2003-08-06 |
CN1129656C (en) | 2003-12-03 |
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Legal Events
Date | Code | Title | Description |
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PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20090615 |